5441-54-3 Usage
Chemical Group
2-(2-methylbutan-2-yl)cyclohexan-1-one belongs to the ketone group.
Molecular Weight
The molecular weight of 2-(2-methylbutan-2-yl)cyclohexan-1-one is 182.30 g/mol.
Usage as Flavoring Agent
2-(2-methylbutan-2-yl)cyclohexan-1-one is commonly used as a flavoring agent in the food industry, providing a mild and sweet aroma.
Production of Perfumes
2-(2-methylbutan-2-yl)cyclohexan-1-one is also used in the production of perfumes and fragrances.
Potential Applications
2-(2-methylbutan-2-yl)cyclohexan-1-one has potential applications in the pharmaceutical and cosmetic industries.
Health Hazards
It is important to handle 2-(2-methylbutan-2-yl)cyclohexan-1-one with care, as it may present health hazards if not properly managed.
Check Digit Verification of cas no
The CAS Registry Mumber 5441-54-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,4 and 1 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 5441-54:
(6*5)+(5*4)+(4*4)+(3*1)+(2*5)+(1*4)=83
83 % 10 = 3
So 5441-54-3 is a valid CAS Registry Number.
InChI:InChI=1/C11H20O/c1-4-11(2,3)9-7-5-6-8-10(9)12/h9H,4-8H2,1-3H3
5441-54-3Relevant articles and documents
Lewis Acid Mediated α-Alkylation of Carbonyl Compounds, VII. Regio and Position Specific α-tert-Alkylation of Ketones
Reetz, Manfred T.,Maier, Wilhelm F.,Chatziiosifidis, Ioannis,Giannis, Athanassios,Heimbach, Horst,Loewe, Ursula
, p. 3741 - 3757 (2007/10/02)
Structurally different ketones can be alkylated at the α-position via their silyl enol ethers with tert-alkyl halides in the presence of Lewis acids such as titanium tetrachloride (->27 - 35).Concerning the alkylation agent, the position specific introduction of branched and cyclic tert-alkyl groups is possible (->41 - 49).Bridgehead halides of the type 1-adamantyl bromide react analogously (->52 - 61).Silyl enol ethers derived from unsymmetrical ketones react regiospecifically (->63, 64, 66, 67).If the reaction partners contain additional functional groups such as aryl residues (->68, 69) or ester groups (->71) or primary alkyl halides moieties (->73), selectivity in the desired manner is observed. α,α'-Bis-tert-alkylated ketones (74 - 76) are also easily accessible, but not the α,α-isomers.
